Morphological and biochemical characterization of primary culture of rabbit proximal kidney tubule cells grown on collagen-IV coated millicell-cm

1997 ◽  
Vol 33 (9) ◽  
pp. 692-702 ◽  
Author(s):  
Isabelle Genestie ◽  
Jean-Paul Morin ◽  
Christophe Guery ◽  
Gerd Bode ◽  
Giocondo Lorenzon
Keyword(s):  
Primary Culture ◽  
Biochemical Characterization ◽  
Collagen Iv ◽  
Kidney Tubule ◽  
Tubule Cells ◽  
Proximal Kidney Tubule

Biochemical, functional, and morphological characterization of a primary culture of rabbit proximal tubule cells

1991 ◽  
Vol 194 (1) ◽  
pp. 9-18 ◽  
Author(s):  
Hervé Toutain ◽  
Nicole Vauclin-Jacques ◽  
Jean-Paul Fillastre ◽  
Jean-Paul Morin
Keyword(s):  
Proximal Tubule ◽  
Primary Culture ◽  
Morphological Characterization ◽  
Proximal Tubule Cells ◽  
Tubule Cells

Plant Pathology Diagnosed by X-Ray Microanalysis

1987 ◽  
Vol 45 ◽  
pp. 974-975
Author(s):  
J. H. Resau ◽  
N. Howell ◽  
S. H. Chang
Keyword(s):  
Electron Microscopy ◽  
Plant Pathology ◽  
Biochemical Characterization ◽  
Nutrient Deficiency ◽  
Green Leaf ◽  
Parasitic Infestation ◽  
X Ray

Spinach grown in Texas developed “yellow spotting” on the peripheral portions of the leaves. The exact cause of the discoloration could not be determined as there was no evidence of viral or parasitic infestation of the plants and biochemical characterization of the plants did not indicate any significant differences between the yellow and green leaf portions of the spinach. The present study was undertaken using electron microscopy (EM) to determine if a micro-nutrient deficiency was the cause for the discoloration.Green leaf spinach was collected from the field and sent by express mail to the EM laboratory. The yellow and equivalent green portions of the leaves were isolated and dried in a Denton evaporator at 10-5 Torr for 24 hrs. The leaf specimens were then examined using a JEOL 100 CX analytical microscope. TEM specimens were prepared according to the methods of Trump et al.

Partial Characterization of a Fibrinolytic Inhibitor Produced by Cultured Endothelial Cells Derived from Human Umbilical Vein

1982 ◽  
Vol 47 (02) ◽  
pp. 128-131 ◽  
Author(s):  
F Esnard ◽  
E Dupuy ◽  
A M Dosne ◽  
E Bodevin
Keyword(s):  
Endothelial Cells ◽  
Primary Culture ◽  
Ammonium Sulphate ◽  
Concanavalin A ◽  
Umbilical Vein ◽  
Human Umbilical Vein ◽  
Preliminary Characterization ◽  
Umbilical Vein Endothelial Cells ◽  
Ammonium Sulphate Saturation

SummaryA preliminary characterization of a fibrinolytic inhibitor released by human umbilical vein endothelial cells in primary culture is reported. This molecule of Mr comprised between 2 × 105 and 106 and of μ2 mobility precipitates at 43% ammonium sulphate saturation and is totally adsorbed on Concanavalin A Sepharose 4 B. A possible relationship with a macroglobulins is discussed.

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